Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205106

From SNPedia

Orientationminus
Geno Mag Summary
(CCTGTATATTCTTAAG;CCTGTATATTCTTAAG) 0 common in clinvar
Make rs786205106(-;-)
Make rs786205106(-;CCTGTATATTCTTAAG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position115740794
GeneCASQ2
is asnp
is mentioned by
dbSNPrs786205106
ebirs786205106
HLIrs786205106
Exacrs786205106
Varsomers786205106
Maprs786205106
PheGenIrs786205106
hapmaprs786205106
1000 genomesrs786205106
hgdprs786205106
ensemblrs786205106
gopubmedrs786205106
geneviewrs786205106
scholarrs786205106
googlers786205106
pharmgkbrs786205106
gwascentralrs786205106
openSNPrs786205106
23andMers786205106
23andMe allrs786205106
SNP Nexus

SNPshotrs786205106
SNPdbers786205106
MSV3drs786205106
GWAS Ctlgrs786205106
Max Magnitude0
ClinVar
Risk rs786205106(;)
Alt rs786205106(;)
Reference rs786205106(CCTGTATATTCTTAAG;CCTGTATATTCTTAAG)
Significance Pathogenic
Disease Ventricular tachycardia not provided
Variation info
Gene CASQ2
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 2 not provided
Reversed 1
HGVS NC_000001.10:g.116283415_116283430del16
CLNSRC OMIM Allelic Variant
CLNACC RCV000019177.28, RCV000170902.2,